1872-69-1 Usage
Uses
Used in Medicinal Chemistry Research:
6-Bromo-8-methyl-3,4-dihydroquinolin-2(1H)-one is used as a research compound for exploring its pharmacological properties. The presence of the bromine and methyl groups allows for the investigation of structure-activity relationships and the compound's interaction with biological targets, which is crucial for the development of new drugs.
Used in Drug Development:
In the pharmaceutical industry, 6-Bromo-8-methyl-3,4-dihydroquinolin-2(1H)-one is utilized as a lead compound in the discovery and optimization of new therapeutic agents. Its unique structure and functional groups make it a promising candidate for further chemical modifications aimed at enhancing its pharmacological efficacy and selectivity.
Used in Chemical Synthesis:
6-Bromo-8-methyl-3,4-dihydroquinolin-2(1H)-one serves as a key intermediate in the synthesis of various complex organic molecules and pharmaceuticals. Its reactive functional groups facilitate multiple synthetic pathways, enabling the production of a wide range of derivative compounds with diverse applications.
Used in Biochemical Assays:
6-Bromo-8-methyl-3,4-dihydroquinolin-2(1H)-one is also employed in biochemical assays to evaluate its binding affinity, selectivity, and potential inhibitory or activating effects on specific enzymes or receptors. Such assays are essential for understanding the mechanism of action and the therapeutic potential of 6-Bromo-8-methyl-3,4-dihydroquinolin-2(1H)-one.
Used in Drug Screening:
6-Bromo-8-methyl-3,4-dihydroquinolin-2(1H)-one is utilized in high-throughput screening processes to identify its potential as a therapeutic agent against various diseases. Its evaluation against a panel of biological targets helps in prioritizing compounds for further development and optimization.
Used in Toxicological Studies:
To ensure the safety and efficacy of 6-Bromo-8-methyl-3,4-dihydroquinolin-2(1H)-one as a potential drug candidate, it is subjected to toxicological studies. These studies assess the compound's potential adverse effects, dose-response relationships, and safety margins, which are critical for its progression to clinical trials and eventual use in patients.
Check Digit Verification of cas no
The CAS Registry Mumber 1872-69-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,7 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1872-69:
(6*1)+(5*8)+(4*7)+(3*2)+(2*6)+(1*9)=101
101 % 10 = 1
So 1872-69-1 is a valid CAS Registry Number.
1872-69-1Relevant academic research and scientific papers
N-SUBSTITUTED BICYCLIC LACTAMS, THEIR PREPARATION AND THEIR USE AS PHARMACEUTICALS
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Page/Page column 66, (2017/03/08)
This application relates to N-substituted bicyclic lactams of formula (I), compositions comprising them and their uses in the treatment of diseases and conditions in which inhibition of a bromodomain is indicated. For example, the application relates to t
